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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

142 related items for PubMed ID: 14209691

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  • 2. MENTAL RETARDATION AND ABNORMAL AMINOACIDURIAS OCCURRING IN A FAMILY.
    ANYON CP.
    N Z Med J; 1965 Jan; 64():3-7. PubMed ID: 14259628
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  • 6. Genetic screening.
    Levy HL.
    Adv Hum Genet; 1973 Jan; 4():1-104. PubMed ID: 4593296
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  • 7. BIOCHEMICAL INVESTIGATION OF HISTIDINAEMIA.
    HOLTON JB, LEWIS FJ, MOORE GR.
    J Clin Pathol; 1964 Nov; 17(6):671-5. PubMed ID: 14227438
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  • 8. MAPLE SYRUP DISEASE AND OTHER RARE DISORDERS OF AMINO ACID METABOLISM.
    MENKES JH.
    Clin Proc Child Hosp Dist Columbia; 1964 Jun; 20():152-60. PubMed ID: 14156868
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  • 11. A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
    EFRON ML, YOUNG D, MOSER HW, MACCREADY RA.
    N Engl J Med; 1964 Jun 25; 270():1378-83. PubMed ID: 14152868
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  • 14. Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.
    Levy HL, Barkin E.
    J Lab Clin Med; 1971 Oct 25; 78(4):517-23. PubMed ID: 5114049
    [No Abstract] [Full Text] [Related]

  • 15. Clearance of toxic metabolites during therapy for inborn errors of metabolism.
    Ring E, Zobel G, Stöckler S.
    J Pediatr; 1990 Aug 25; 117(2 Pt 1):349-50. PubMed ID: 2380843
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  • 16. MAPLE SYRUP URINE DISEASE, WITH PARTICULAR REFERENCE TO DIETOTHERAPY.
    SNYDERMAN SE, NORTON PM, ROITMAN E, HOLT LE.
    Pediatrics; 1964 Oct 25; 34():454-72. PubMed ID: 14212461
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  • 17. Aminoacidurias due to inherited disorders of metabolism. 2.
    Frimpter GW.
    N Engl J Med; 1973 Oct 25; 289(17):895-901. PubMed ID: 4598151
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  • 18. Diagnostic challenges of aminoacidopathies and organic acidemias in a developing country: a twelve-year experience.
    Karam PE, Habbal MZ, Mikati MA, Zaatari GE, Cortas NK, Daher RT.
    Clin Biochem; 2013 Dec 25; 46(18):1787-92. PubMed ID: 23994778
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  • 19. MAPLE SYRUP URINE DISEASE. REPORT OF THE FIRST CASE IN PUERTO RICO.
    JIMENEZ AI, SIFONTES JE, SANCHEZLONGO LP.
    Bol Asoc Med P R; 1963 Nov 25; 55():463-8. PubMed ID: 14112942
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  • 20. THE PRIMARY AMINO-ACIDOPATHIES. GENETIC DEFECTS IN THE METABOLISM OF THE AMINO ACIDS.
    DIGEORGE AM, AUERBACH VH.
    Pediatr Clin North Am; 1963 Aug 25; 10():723-44. PubMed ID: 14145016
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